Hierarchical nanoassembly of Ni3S2-MoS2 interconnected with CeO2 as a highly remarkable hybrid electrocatalyst for enhancing water oxidation and energy storage

电催化剂 塔菲尔方程 超级电容器 析氧 材料科学 电化学 化学工程 循环伏安法 催化作用 分解水 储能 纳米技术 化学 电极 物理化学 有机化学 功率(物理) 热力学 工程类 物理 光催化
作者
Mrunal Bhosale,Nimisha Baby,Sahil S. Magdum,Nagaraj Murugan,Yoong Ahm Kim,Sadhasivam Thangarasu,Tae Hwan Oh
出处
期刊:Journal of energy storage [Elsevier BV]
卷期号:80: 110301-110301 被引量:8
标识
DOI:10.1016/j.est.2023.110301
摘要

Emerging earth-abundant multifunctional electrocatalysts with highly efficient performance are important substitutes for replacing the expensive noble metal catalysts to attain sustainable electrochemical water splitting and supercapacitor applications. Therefore, we developed a well-interconnected Ni3S2-MoS2-CeO2 (NMC) nanostructure as a multifunctional electrocatalyst for the utilization in dual purposes, mainly energy conversion and storage applications. In alkaline conditions, the NMC-1 exhibits remarkable oxygen evolution reaction (OER) performances of lower over potential (206.03 mV at 10 mA/cm2) coupled with the lowest Tafel slope (40.19 mV·dec−1). The NMC-1 further shows excellent stability, where the durability of the electrocatalyst was verified after a considerable number of cyclic voltammetry (5000 cycles) and chronopotentiometry. The coexistence of the Ce3+ and Ce4+ oxidation states generates a favorable environment for surface oxygen ion exchange. The inherent stability of CeO2 facilitates a strong and intimate electrochemical coupling with NiOOH. This synergistic interaction between CeO2, MoS2, and NiOOH further enhances the performance of the catalytic system. Notably, the hybrid structure of NMC-1 exhibited superior supercapacitor performance (417 F/g at 1 A/g). The fabricated asymmetric supercapacitor device showed efficient performance by attaining a high energy density of 4.84 Wh kg−1 at a power density of 72 W kg−1. According to the intrinsic properties of each material in NMC and the existence of synergy owing to the outstanding interfacial contact between the compounds in NMC, reasonably abundant surface-active sites are available for attaining rapid charge transfer, enhancing the inherent activity and durability of the catalyst, which is the key reason for better OER and supercapacitor performance. This study provides useful understandings into the strategic design of advanced multifunctional electrode materials for next-generation applications.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
1秒前
2秒前
2秒前
SDUMoist发布了新的文献求助10
2秒前
高高梦松发布了新的文献求助10
3秒前
mlr完成签到,获得积分20
3秒前
俊逸元正完成签到,获得积分20
4秒前
小汪快跑发布了新的文献求助10
4秒前
斯文败类应助tangxinhebaodan采纳,获得10
5秒前
量子星尘发布了新的文献求助10
5秒前
5秒前
樱桃小浣发布了新的文献求助10
5秒前
6秒前
6秒前
BeLoved发布了新的文献求助10
7秒前
asuan发布了新的文献求助10
7秒前
andy发布了新的文献求助10
7秒前
俊逸元正发布了新的文献求助10
7秒前
10秒前
单薄靖儿发布了新的文献求助10
10秒前
10秒前
11秒前
12秒前
汉堡包应助刻苦的媚颜采纳,获得10
13秒前
qscheng发布了新的文献求助10
13秒前
14秒前
学习学习学习完成签到,获得积分10
14秒前
李爱国应助fine采纳,获得10
14秒前
SciGPT应助Han采纳,获得10
14秒前
jiang发布了新的文献求助10
14秒前
LEI发布了新的文献求助10
16秒前
无奈的碧彤完成签到,获得积分10
16秒前
觅莲者乙丑完成签到,获得积分10
17秒前
李健应助舒适尔容采纳,获得10
17秒前
科研通AI6.4应助zy采纳,获得10
19秒前
19秒前
20秒前
21秒前
打打应助单薄靖儿采纳,获得10
22秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Burger's Medicinal Chemistry, Drug Discovery and Development, Volumes 1 - 8, 8 Volume Set, 8th Edition 1800
Cronologia da história de Macau 1600
Contemporary Debates in Epistemology (3rd Edition) 1000
International Arbitration Law and Practice 1000
文献PREDICTION EQUATIONS FOR SHIPS' TURNING CIRCLES或期刊Transactions of the North East Coast Institution of Engineers and Shipbuilders第95卷 1000
BRITTLE FRACTURE IN WELDED SHIPS 1000
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 纳米技术 计算机科学 化学工程 生物化学 物理 复合材料 内科学 催化作用 物理化学 光电子学 细胞生物学 基因 电极 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6156258
求助须知:如何正确求助?哪些是违规求助? 7984771
关于积分的说明 16593133
捐赠科研通 5266286
什么是DOI,文献DOI怎么找? 2810027
邀请新用户注册赠送积分活动 1790261
关于科研通互助平台的介绍 1657564